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HRID 1619099作成日:2026年10月27日

N,N,N',N'-Tetramethylethylenediamine → 6'-Bromospiro[cyclopentane-1,3'-indolin]-2'-one

https://huagongshe.com/reaction/1619099

反応式

関与物質

役割名称HCID仕込み量
反応物N,N,N',N'-TetramethylethylenediamineHCID 8037—
反応物1,4-DiiodobutaneHCID 12337—
反応物Ammonium ChlorideHCID 25517—
反応物6-bromo-2,3-dihydro-1H-indol-2-oneHCID 2773289—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物6'-Bromospiro[cyclopentane-1,3'-indolin]-2'-oneHCID 1271709045.6%

反応条件

温度-20 °C

反応手順

n-Butyl lithium (2.5 M in hexanes, 3.8 mL, 9.5 mmol) was added dropwise over 30 minutes to a stirred suspension of 6-bromoindolin-2-one (preparation 1, 1.00 g, 4.7 mmol) and N,N,N′,N′-tetramethylethylenediamine (1.42 mL, 9.4 mmol) in tetrahydrofuran (20 mL) at −78° C. The mixture was stirred for 1 hour, then 1,4-diiodobutane (3.11 mL, 23.6 mmol) was added dropwise over 5 minutes. The mixture was warmed to −20° C. over a 1 hour period, was stirred for a further hour at this temperature and was then warmed to room temperature. After 3 hours stirring at room temperature, saturated aqueous ammonium chloride solution was added to the reaction and the mixture was extracted with ethyl acetate. The organic layer was washed with water, brine, dried (MgSO4) and evaporated. Purification of the residue by flash chromatography (10:1 hexanes/ethyl acetate) gave the title compound (0.57 g, 45%) as a pale pink solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08772288B2
出典データセットuspto-grants-2014_07
ORD IDord-f6b086492ca44bd5bd1fbd33eea48b0c
出典メモuspto-grants-2014_07